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dc.contributor.authorMcKellar, Quintin
dc.contributor.authorGibson, I.
dc.contributor.authorMonteiro, A.
dc.contributor.authorBregante, M.
dc.date.accessioned2014-01-21T16:30:27Z
dc.date.available2014-01-21T16:30:27Z
dc.date.issued1999-08
dc.identifier.citationMcKellar , Q , Gibson , I , Monteiro , A & Bregante , M 1999 , ' Pharmacokinetics of enrofloxacin and danofloxacin in plasma, inflammatory exudate, and bronchial secretions of calves following subcutaneous administration ' , Antimicrobial Agents and Chemotherapy , vol. 43 , no. 8 , pp. 1988-1992 .
dc.identifier.issn1098-6596
dc.identifier.otherPURE: 1417098
dc.identifier.otherPURE UUID: 1a7c16dd-4b99-496c-a848-f5bf107c1fb1
dc.identifier.otherBibtex: urn:cdd4418db0a68a7fde6dc9f4d410780d
dc.identifier.otherScopus: 0032840507
dc.identifier.urihttp://hdl.handle.net/2299/12595
dc.description.abstractEnrofloxacin (2.5 mg/kg of body weight) and danofloxacin (1.25 mg/kg) were administered subcutaneously to ruminating calves (n = 8) fitted with subcutaneous tissue cages. Concentrations of enrofloxacin, its metabolite ciprofloxacin, and danofloxacin in blood (plasma), tissue cage exudate (following intracaveal injection of 0.3 mi of 1% [vol/wt] carrageenan), and bronchial secretions were measured by high-performance liquid chromatography (HPLC) and microbiological assay (enrofloxacin plus ciprofloxacin and danofloxacin). Mean maximum concentrations (C-max) +/- standard deviations of enrofloxacin (0.24 +/- 0.08 mu g/ml), ciprofloxacin (0.11 +/- 0.03 [total, 0.34 +/- 0.10] mu g/ml), and danofloxacin (0.23 +/- 0.05 mu g/ml) were detected in the plasma of calves by HPLC. The C-max were 0.49 +/- 0.17 mu g/ml (enrofloxacin equivalents) and 0.24 +/- 0.03 mu g/ml (danofloxacin) when they were measured by microbiological assay. Mean C-max in exudate (HPLC) were 0.18 +/- 0.07 mu g/ml (enrofloxacin), 0.10 +/- 0.04 mu g/ml (ciprofloxacin), 0.27 +/- 0.09 mu g/ml (enrofloxacin plus ciprofloxacin), and 0.19 +/- 0.05 mu g/ml (danofloxacin), and concentrations in exudate exceeded those in plasma from 8 h (enrofloxacin and ciprofloxacin) or 6 h (danofloxacin) after drug administration. The C-max were 0.34 +/- 0.09 mu g/ml (enrofloxacin equivalents) and 0.22 +/- 0.04 mu g/ml (danofloxacin) in exudate when they were measured by the microbiological assay. The maximum mean concentration achieved in bronchial secretions (HPLC) were 0.07 +/- 0.04 mu g/ml (enrofloxacin), 0.04 +/- 0.07 mu g/ml (ciprofloxacin), 0.10 +/- 0.05 mu g/ml (enrofloxacin plus ciprofloxacin), and 0.12 +/- 0.09 mu g/ml (danofloxacin). The maximum mean concentration in bronchial secretions from a limited number of animals from which samples were available for microbiological assay were 0.27 +/- 0.11 mu g/ml (n = 4 [enrofloxacin equivalents]) and 0.14 +/- 0.02 mu g/ml (n = 3 [danofloxacin]). With predictive models of efficacy (C-max/MIC and area under the concentration-time curve/MIC ratios in plasma) for Pasteurella multocida (MIC of enrofloxacin, 0.06 mu g/ml [24]; MIC of danofloxacin, 0.06 mu g/ml [6]), enrofloxacin produced scores of 8.17 and 52.00, respectively, compared to those of danofloxacin, which were 4.02 and 23.05, respectively. With the dosing rates recommended in some markets by manufacturers, enrofloxacin and danofloxacin achieved concentrations above the MICs for important pathogenic organisms in plasma, tissue cage exudate, and bronchial secretion. Since fluoroquinolones display concentration-dependent activities, C-max/MIC ratios may be critical to efficacy. In the United States enrofloxacin is currently the only fluoroquinolone licensed for food animals and dosages for acute respiratory disease are 2.5 to 5 mg/kg for 3 days or 7.5 to 12.5 mg/kg once. The higher dosages on a single occasion are likely to confer C-max/MIC ratios that are associated with greater clinical efficacy.en
dc.format.extent5
dc.language.isoeng
dc.relation.ispartofAntimicrobial Agents and Chemotherapy
dc.subjectCIPROFLOXACIN
dc.subjectEFFICACY
dc.subjectMODEL
dc.subjectDOGS
dc.titlePharmacokinetics of enrofloxacin and danofloxacin in plasma, inflammatory exudate, and bronchial secretions of calves following subcutaneous administrationen
dc.contributor.institutionOffice of the Vice-Chancellor
dc.contributor.institutionVeterinary Science
dc.contributor.institutionGeography, Environment and Agriculture
dc.description.statusPeer reviewed
dc.identifier.urlhttp://aac.asm.org/content/43/8/1988.full.pdf+html
dcterms.dateAccepted1999-08
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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